SCIENTIFIC DISCUSSION

Transcription

1 SCIENTIFIC DISCUSSION This part reflects the scientific knowledge and the information about this product available at the time of prequalification. Thereafter, updates may have become necessary which are included in parts 1 to 5 and, if related to pharmaceutical issues, also documented in part 8 of this WHOPAR. Name of the Finished Pharmaceutical Product: Manufacturer of PreQualified Product: Active Pharmaceutical Ingredient (API): International Nonproprietary Name: Pharmaco-therapeutic group (ATC Code): Therapeutic indication: 100 mg Tablets * Macleods Pharmaceutical Limited Plot No , Survey No. 366 Premier Industrial Estate Kachigam, Daman (UT) India Antimycobacterials, hydrazides (J04AC01) 100 mg Tablets is indicated for the treatment of tuberculosis, caused by Mycobacterium tuberculosis. * Trade names are not prequalified by WHO. This is under local DRA responsibility. Throughout this WHOPAR the proprietary name is given as an example only. Page 1 of 5

2 1. Introduction 100 mg Tablets is indicated for the treatment of tuberculosis, caused by Mycobacterium tuberculosis. is not indicated for use in patients with clinically significant hypersensitivity to isoniazid or to any of the components contained in the formulation. It is recommended that therapy is given only on the advice of a tuberculosis experienced physician. 2 Assessment of Quality Active pharmaceutical Ingredient (API) is a class 3/1 API according to Biopharmaceutics Classification System (WHO Technical Report Series 937, Annex 8: Proposal to waive in vivo bioequivalence requirements for WHO Model List of Essential Medicines immediate-release, solid oral dosage forms). is described in the Ph.Int., Ph.Eur. and the USP and is considered well-established. The API, which is obtained from approved API manufacturer, is adequately controlled by quality specifications which are pharmacopoeial based, with an additional in-house specification for residual solvents. Based on the results of stability testing conducted according to the requirements of WHO, a retest period of 5 years was approved for isoniazid. Other ingredients Other ingredients used in the tablet formulation include calcium hydrogen phosphate, colloidal anhydrous silica, disodium edetate, magnesium stearate, maize starch and purified talc, which are all compendial. Magnesium stearate is of vegetable origin. Finished pharmaceutical product (FPP) Pharmaceutical development tablets are described in the Ph.Int., BP and USP and are considered well- established. 100 mg Tablets are white, circular, biconvex, uncoated tablets having plain surface on both the sides. The tablets (1,000) are packed in an LDPE bag, which is further packed in a round, white opaque HDPE jar, tagger-sealed with an aluminium circular foil (soft tempered) laminated with LDPE film and closed with a polypropylene screw cap. The tablets are also presented in plain aluminium foil/white opaque PVDC coated PVC blister cards of 10 tablets. The development of the final composition of 100mg Tablets has been described and the compatibility of the API with the excipients demonstrated. The manufacturing process entails a conventional wet granulation followed by drying, lubrication, compression and packaging. Appropriate in-process controls have been set to ensure batch-to-batch reproducibility. Validation data presented on three production batches and batch analysis data demonstrate the consistency of the process and the quality of the product. The pharmacopoeial based specifications and analytical methods with validation are considered adequate for controlling the quality of this finished pharmaceutical product at release and during shelf life. The dissolution profiles of 100 mg Tablets and 300mg Tablets (the latter being the test product, used in bioequivalence studies) in all three BCS media were demonstrated to be similar, and this was also the basis of the biowaiver allowed for 100 mg Tablets. The two strengths are proportionally similar with respect to composition. Page 2 of 5

3 Stability testing Stability studies have been performed at 30 C/70%RH as long-term conditions and at accelerated conditions according to the requirements of WHO. At the time of the prequalification, a shelf-life of 24 months has been allowed for the FPP when stored at a temperature not above 30 C. The applicant committed to continue long-term testing on production scale batches for a period of time sufficient to cover the whole proposed shelf-life and to report any out-of-specification results immediately to WHO. Conclusions The quality part of the dossier is accepted. 3. Assessment of Bio-Equivalence The following bioequivalence study has been performed in 2005 according to internationally accepted guidelines. An open label, randomized, two-treatment, two sequence, two period, two way crossover, single dose bioequivalence study of BP 300 mg tablets manufactured by Macleods Pharmaceuticals Ltd., India comparing with three tablets of Isozid 100 mg (each containing isoniazid 100 mg) of Fatol Arzneimittel GmbH, Schiffweiler, Germany, in healthy, adult, male, human subjects under fasting conditions (study no. BEQ-009-ISON-2005). The objective of the study was to compare the bioavailability of the stated isoniazid 300 mg tablet manufactured by Macleods Pharmaceuticals Ltd., India (test drug) with the same dose of the reference tablet (Isozid, Fatol Arzneimittel) and to assess bioequivalence. The comparison was performed as a single centre, open label, randomized, crossover study in healthy subjects under fasting conditions. Each subject was assigned to receive each of the following two treatments in a randomized fashion: Treatment T: Treatment R: Test BP 300 mg tablet (isoniazid 300 mg) Batch no. IB501. Reference 3 x Isozid 100 mg tablet (isoniazid 100 mg) Batch no A 7 day wash-out period was observed between administration of test and references. Serial blood samples (1 pre-dose sample and 16 samples within 24 h post dose) were taken during each study period to obtain bioavailability characteristics AUC, C max and t max for bioequivalence evaluation. Drug concentrations for isoniazid were analyzed using a validated HPLC method. The limit of quantification was stated to be about 100 ng/ml for isoniazid. The study was performed with 28 participants; data generated from a total of 24 subjects were utilized for analysis to establish pharmacokinetic parameters and assess bioequivalence. Arithmetic mean and geometric mean values of the pharmacokinetic variables for isoniazid as well as statistical results are summarised in the following tables: Page 3 of 5

4 Pharmacokinetic Parameter Test formulation (T) arithmetic mean ± SD (*) Reference (R) arithmetic mean ± SD (*) log-transformed parameters Ratio Conventional T/R (%) 90% CI (ANOVAlog) t max (h) 0.68 ± ± C max (µg/ml) 7.27 ± ± (7.05) (6.79) AUC 0-t (µg.h/ml) ± ± (29.30) (28.82) AUC 0-inf (µg.h/ml) ± ± (30.33) (29.69) * geometric mean Conclusions: The results of the study show that preset acceptance limits of % are met by both AUC and C max values regarding isoniazid. Accordingly, the test tablet BP 300 mg meets the criteria for bioequivalence with regard to rate and extent of absorption and is therefore bioequivalent to the reference Isozid (Fatol Arzneimittel). A biowaiver was granted for the additional strength 100 mg Tablets (isoniazid 100 mg, Macleods Pharmaceuticals Ltd., India) in accordance to the WHO guideline. In comparison with the strength of the test product used in the bioequivalence study, the 100 mg strength was determined to be qualitatively essentially the same, the ratio of active ingredients and excipients between the strengths is considered essentially the same, and the dissolution profiles between the formulations for the three APIs in three media (0.1N HCl, ph buffer 4.5 and ph buffer 6.8) were determined to be similar. 4. Summary of Product Safety and Efficacy Background 100 mg Tablets has been shown to conform to the same appropriate standards of quality, efficacy and safety as those required of the innovator`s product. According to the submitted data on quality and bioavailability it is pharmaceutically and therapeutically equivalent to the reference, Isozid (isoniazid 100 mg tablets). The clinical safety of this product is considered to be acceptable when guidance and restrictions presented in the Summary of Product Characteristics are taken into consideration. Reference is made to the SPC (WHOPAR part 4) for data on clinical safety. 5. Benefit risk assessment and overall conclusion Quality The quality of this product is considered to be acceptable when used in accordance with the conditions defined in the SPC. Physicochemical and biological aspects relevant to the uniform clinical performance of the product have been investigated and are controlled in a satisfactory way. Bioequivalence 100 mg Tablets fulfilled all criteria for waiving an in-vivo bioequivalence study as per relevant WHO guidance. Hence, it is concluded on bioequivalence between 100 mg Tablets and Isozid 100 mg tablet (Fatol Arzneimittel). Page 4 of 5

5 Efficacy and Safety Regarding clinical efficacy and safety, 100 mg Tablets are considered effective and safe to use when the guidance and restrictions presented in the Summary of Product Characteristics is taken into consideration. Benefit Risk Assessment Based on the WHO assessment of data on quality, bioequivalence, safety and efficacy the team of assessors considered by consensus that the benefit risk profile of 100 mg Tablets was acceptable for the following indication: treatment of tuberculosis caused by Mycobacterium tuberculosis and has advised to include 100 mg Tablets, manufactured at Macleods Pharmaceutical Limited, Plot No , Survey No. 366, Premier Industrial Estate, Kachigam, Daman (UT), India in the list of pre-qualified medicinal products. Page 5 of 5